EP2493605A1 - Designed mixed metal oxide ingredients for bulk metal oxide catalysts - Google Patents
Designed mixed metal oxide ingredients for bulk metal oxide catalystsInfo
- Publication number
- EP2493605A1 EP2493605A1 EP10827521A EP10827521A EP2493605A1 EP 2493605 A1 EP2493605 A1 EP 2493605A1 EP 10827521 A EP10827521 A EP 10827521A EP 10827521 A EP10827521 A EP 10827521A EP 2493605 A1 EP2493605 A1 EP 2493605A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- metal oxide
- catalyst
- mixed metal
- bulk
- designed mixed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/007—Mixed salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/002—Mixed oxides other than spinels, e.g. perovskite
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/005—Spinels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/881—Molybdenum and iron
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/887—Molybdenum containing in addition other metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/8871—Rare earth metals or actinides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/887—Molybdenum containing in addition other metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/8872—Alkali or alkaline earth metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/888—Tungsten
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/04—Mixing
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3332—Catalytic processes with metal oxides or metal sulfides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
- C07C2523/56—Platinum group metals
- C07C2523/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tatalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/652—Chromium, molybdenum or tungsten
Definitions
- the present invention generally relates to bulk metal oxide catalysts used in the conversion of hydrocarbons.
- Bulk metal oxide catalysts generally include multiple metal oxide components. Numerous examples of bulk metal oxide catalysts are well known in the art and are generally used for the conversion of hydrocarbons. For instance, bulk metal oxide catalysts are known in the processes of desulfurization, oxidation, ammoxidation, and dehydrogenation, just to name a few.
- a bulk metal oxide catalyst is a dehydrogenation catalyst having metal oxides of Fe, K, and Ce.
- This catalyst can be used in the conversion of alkylaromatic hydrocarbons to alkenylaromatic hydrocarbons, such as the conversion of ethylbenzene to styrene.
- this catalyst can include numerous promoters, generally in the form of other metal oxides, intended to enhance the physical and/or chemical properties of the catalyst.
- bulk metal oxide catalysts are prepared by combining individual metal oxide powders, mixing, processing, and then calcining the mixture at high temperatures from about 500°C to 1000°C. There is generally little specificity in the order or groupings in which the ingredients are combined.
- desired mixed metal oxide phases and modified metal oxide phases are difficult to predict and/or control in the processing of separate metal oxide ingredients. This unpredictability associated with bulk metal oxide catalyst preparation can be aggravated by the addition of other metal oxide promoters that are detrimental to the formation of desired mixed phases.
- potassium ferrite phases are known to form in dehydrogenation catalysts during heat treatment and are generally desirable. Certain promoters, such as those intended to enhance the iron oxide phase or to improve physical properties, can adversely affect the formation of the potassium ferrite phases.
- Embodiments of the present invention involved the use of designed mixed metal oxide ingredients in the preparation of bulk metal oxide catalysts.
- Designed mixed metal oxide ingredients include one or more metal oxides or metal oxides precursors that are combined and reacted prior to their inclusion in the formulation of the catalyst.
- a metal oxide or metal oxide precursor can be any metal compound known in the art as a bulk metal oxide catalyst ingredient.
- a metal compound can be chosen from the group consisting of Groups I - VIA and I-VIIIB of the periodic table, and the rare earth metals.
- the designed mixed metal oxide includes at least two of these metal compounds and can have several, in varying combinations in an oxide form.
- the invention is for a bulk metal oxide catalyst that includes among its ingredients a designed mixed metal oxide.
- the invention is a method of preparing a bulk metal oxide catalyst that includes combining and reacting selected ingredients to form a designed mixed metal oxide, combining said designed mixed metal oxide with other catalyst ingredients, shaping, drying, and calcining the mixture.
- the bulk metal oxide catalyst can be any known in the art.
- the catalyst can be one that is used in the conversion of alkylaromatic compounds to alkenylaromatic compounds, such as the conversion of ethylbenzene to styrene.
- Figure 1 is a graph of Styrene Selectivity versus EB Conversion for EB to styrene conversions using the catalyst produced in comparative Batch 2.
- the present invention provides greater specificity in the preparation of bulk metal oxide catalysts through the use of designed mixed metal oxide ingredients.
- Designed mixed metal oxide ingredients include selected catalyst ingredients that are separately prepared and reacted prior to their being added to the catalyst formulation.
- the invention is for a method of preparing a bulk metal oxide catalyst. Instead of simultaneously mixing all singular ingredients for the catalyst, selected ingredients are pre-mixed and pre -reacted. The pre-reacted ingredients form a designed mixed metal oxide that can then be added to the other catalyst ingredients to ensure that the desired mixed metal phase is in the finished catalyst.
- the bulk metal oxide catalyst can then be mixed, reacted, shaped, dried, and calcined according to conventional methods known in the art.
- the designed mixed metal oxide includes a bulk metal oxide catalyst ingredient combined with one or more other metal oxides that affect the properties that the ingredient imparts to the catalyst.
- ingredients When some ingredients are used individually as an ingredient in a catalyst, they can produce poor results. Instead, such ingredients can be modified with one or more other metal oxides to create a new ingredient and ultimately an improved catalyst.
- the ingredient and the other metal oxides can be mixed and reacted until a desired mixed metal oxide phase is produced.
- the designed mixed metal oxide can have new chemical and physical properties, and can be considered a new ingredient for the preparation of a bulk metal oxide catalyst.
- the designed mixed metal oxide includes a bulk metal oxide catalyst ingredient combined with one or more other metal oxides that affect the ingredient's stability.
- Some ingredients can have poor stability when used as an individual ingredient as a catalyst. The poor stability can manifest itself in the ingredient being volatile at reactor conditions or being easily lost from the catalyst over time.
- Such ingredients can be modified with one or more other metal oxides to create a stabilized ingredient.
- the ingredient and the one or more other metal oxides can be mixed and reacted until a desired mixed metal oxide phase is produced.
- the designed mixed metal oxide can have new properties, such as greater stability, when used in the preparation of a bulk metal oxide catalyst.
- potassium an ingredient commonly included in the formulations of styrene catalysts
- potassium can be volatile at reactor conditions and can be easily lost during a catalyst run, thereby deactivating the styrene catalyst.
- Potassium can instead be combined with a support material such as alumina before being used in a styrene catalyst preparation.
- the modified potassium can exhibit greater stability and can, in turn, increase the life of the styrene catalyst.
- the designed mixed metal oxide can be a mixed metal oxide co-catalyst.
- the co-catalyst can be prepared according to conventional methods known in the art and can then be used as an ingredient in the preparation of a bulk metal oxide catalyst.
- the co-catalyst can enhance the chemical and physical properties of the bulk metal oxide catalyst.
- Examples of mixed metal co-catalysts that can be used include water gas shift catalysts, oxidation catalysts, dehydrogenation catalysts, de-coking catalysts, and catalysts for hydrogen transfer reactions.
- potassium aluminate can be used in the preparation of a styrene catalyst to enhance de-coking.
- the designed mixed metal oxide can be a specialized ingredient that can only be added to the bulk metal oxide catalyst formulation by separate preparation, then subsequent addition as a catalyst ingredient.
- specialized ingredients can be added to affect the chemical and/or physical properties of the bulk metal oxide catalyst.
- beta aluminates are platelike crystals that can have high temperature stability and high porosity. They can be used in bulk metal oxide catalysts, such as styrene catalysts. Beta aluminates are generally formed by combining alkali metals with alumina and calcining the mixture at high temperatures.
- Other specialized ingredients can be prepared according to the procedure known in the art and used as ingredients in the preparation of bulk metal oxide catalysts.
- the designed mixed metal oxide ingredients can be used in the formulation of any bulk metal oxide catalyst known in the art.
- Bulk metal oxide catalysts are used for a variety of processes, such as desulfurization, oxidation, ammoxidation, and dehydrogenation, just to name a few.
- the present invention can be useful for any bulk metal oxide catalyst that benefits from greater specificity in its preparation, regardless of its intended use.
- One bulk metal oxide catalyst for which this invention is useful is a catalyst for the dehydrogenation of alkylaromatics to alkenylaromatics.
- a catalyst for the dehydrogenation of alkylaromatics to alkenylaromatics is a styrene catalyst that promotes the conversion of ethylbenzene to styrene.
- Such catalysts are generally prepared by mixing iron oxide, potassium oxide, cerium oxide, and other ingredients. The mixture is then shaped, dried, calcined, and placed in a reactor.
- Dehydrogenation reactions can take place, in one non-limiting example, at a temperature of from 540°C to 660°C, a pressure in the range of sub-atmospheric to around atmospheric pressure, and a LHSV of from 0.1 fir " 1 to 5 hr "1 .
- Designed mixed metal oxides that can be used in the present invention include at least one metal oxide or one metal oxide precursor.
- a metal oxide precursor forms an oxide phase at high temperatures, such as those used in calcining.
- a metal oxide or metal oxide precursor can be any metal compound known in the art as a bulk metal oxide catalyst ingredient.
- a metal compound can be selected from the group consisting of Groups I-VIA, I-VIIIB, of the periodic table and the rare earth metals.
- the designed mixed metal oxide includes at least one of these metal compounds and can have several, in varying combinations.
- a bulk metal oxide catalyst according to the present invention contains from 0.1 to 85 wt% of a designed mixed metal oxide, optionally from 1.0 to 75 wt%, optionally from 5.0 to 50 wt%, optionally from 10.0 to 40 wt%.
- the other catalyst ingredients can include conventional ingredients known in the art as well as any promoters and/or stabilizers that affect physical and/or chemical properties.
- a bulk metal oxide catalyst was prepared by combining a pre-formed mixed metal oxide, magnesium aluminate, with other ingredients followed by forming and calcination.
- the pre-formed magnesium aluminate amounts to about one quarter of the ingredients by weight.
- the catalyst was prepared by mixing the powdered ingredients, adding water, followed by extruding into formed cylindrical shapes. The final step is a high temperature calcination at 775°C for four hours.
- the ingredient list is shown in Table 1.
- a bulk metal oxide catalyst with similar ingredient percentages but without the pre-formed mixed metal oxide can be used as a comparative example.
- the catalyst was prepared by mixing the powdered ingredients, adding water, followed by extruding into formed cylindrical shapes. The final step was high temperature calcination at 775°C for four hours.
- the ingredient list is shown in Table 1.
- Figure 1 is a graph of Styrene Selectivity versus EB Conversion for EB to styrene conversions using the catalyst produced in Batch 2. Ethylbenzene conversions ranged from about 30% to about 63% while the Styrene Selectivity ranged from about 93% to about 95%.
- catalyst refers to any bulk metal oxide catalyst known in the art, unless explicitly stated otherwise.
- the term "designed mixed metal oxide” refers to any metal oxide or combinations of metal oxides that are mixed and reacted to a desired phase prior to their inclusion in the preparation of a catalyst.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/610,311 US20110105316A1 (en) | 2009-10-31 | 2009-10-31 | Mixed Metal Oxide Ingredients for Bulk Metal Oxide Catalysts |
| PCT/US2010/054680 WO2011053770A1 (en) | 2009-10-31 | 2010-10-29 | Designed mixed metal oxide ingredients for bulk metal oxide catalysts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2493605A1 true EP2493605A1 (en) | 2012-09-05 |
| EP2493605A4 EP2493605A4 (en) | 2013-05-15 |
Family
ID=43922575
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10827521.5A Withdrawn EP2493605A4 (en) | 2009-10-31 | 2010-10-29 | Designed mixed metal oxide ingredients for bulk metal oxide catalysts |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20110105316A1 (en) |
| EP (1) | EP2493605A4 (en) |
| JP (1) | JP2013509297A (en) |
| CN (1) | CN102596394A (en) |
| TW (1) | TW201130558A (en) |
| WO (1) | WO2011053770A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110105818A1 (en) * | 2009-10-31 | 2011-05-05 | Fina Technology, Inc. | Dehydrogenation Catalyst with a Water Gas Shift Co-Catalyst |
| CN112657503B (en) * | 2019-10-15 | 2023-09-29 | 中国石油化工股份有限公司 | Iron-based catalyst and preparation method and application thereof |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3387053A (en) * | 1965-11-12 | 1968-06-04 | Monsanto Co | Dehydrogenation catalyst and process |
| US4710484A (en) * | 1982-06-25 | 1987-12-01 | The Standard Oil Company | Method for preparing a supported mixed-metal oxide oxidation catalyst |
| US4975267A (en) * | 1987-06-25 | 1990-12-04 | Columbian Chemicals Co. | Stable K2 FE22 O34 potassium ferrite phase and method of manufacture |
| US5023225A (en) * | 1989-07-21 | 1991-06-11 | United Catalysts Inc. | Dehydrogenation catalyst and process for its preparation |
| JPH10510524A (en) * | 1994-12-14 | 1998-10-13 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイ | Large particle dehydrogenation catalyst and method |
| KR100373572B1 (en) * | 1994-12-14 | 2003-04-21 | 쉘 인터내셔널 리써치 마챠피즈 비 브이 | Dehydrogenation catalyst and process |
| EP0797481B1 (en) * | 1994-12-14 | 2000-08-30 | Shell Internationale Researchmaatschappij B.V. | Restructured iron oxide |
| IT1293531B1 (en) * | 1997-08-01 | 1999-03-01 | Sud Chemie Mt S R L Ex Monteca | CATALYSTS FOR DEHYDROGENATION OF ETHYLBENZENE TO STYRENE |
| US6417422B1 (en) * | 1999-02-22 | 2002-07-09 | Symyx Technologies, Inc. | Ni catalysts and methods for alkane dehydrogenation |
| IT1313647B1 (en) * | 1999-09-30 | 2002-09-09 | Snam Progetti | PROCEDURE FOR THE DEHYDROGENATION OF ETHYLBENZENE TO STYRENE. |
| DE10150811A1 (en) * | 2001-10-15 | 2003-04-24 | Basf Ag | Dehydrogenation of alkanes, e.g. propane to propene, comprises dehydrogenation of ethylbenzene to styrene to form hydrogen containing waste gas stream and heterogeneous catalyzed dehydrogenation of the alkane mixed with the hydrogen |
| KR20030072541A (en) * | 2002-03-04 | 2003-09-15 | 한국화학연구원 | Novel Method for Catalytic Dehydrogenation of Hydrocarbons Using Carbon Dioxide as Soft Oxidant |
| NL1020923C2 (en) * | 2002-06-21 | 2003-12-23 | Otb Group Bv | Method and device for manufacturing a catalyst. |
| BRPI0500615B1 (en) * | 2004-03-10 | 2015-07-14 | Rohm And Haas Company | Modified Catalyst and Modified Catalyst System |
| RU2385313C2 (en) * | 2004-11-18 | 2010-03-27 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Improved method of producing alkenyl aromatic compound at low vapour/hydrocarbon ratio |
| US7468465B2 (en) * | 2005-05-31 | 2008-12-23 | Exxonmobil Chemical Patents Inc. | Method of making mixed metal oxide containing sulfur |
| US20100081855A1 (en) * | 2008-09-30 | 2010-04-01 | Fina Technology, Inc. | Semi-Supported Dehydrogenation Catalyst |
| US9539543B2 (en) * | 2009-01-29 | 2017-01-10 | Basf Corporation | Mechanically fused materials for pollution abatement in mobile and stationary sources |
| US20110105818A1 (en) * | 2009-10-31 | 2011-05-05 | Fina Technology, Inc. | Dehydrogenation Catalyst with a Water Gas Shift Co-Catalyst |
-
2009
- 2009-10-31 US US12/610,311 patent/US20110105316A1/en not_active Abandoned
-
2010
- 2010-09-30 TW TW099133327A patent/TW201130558A/en unknown
- 2010-10-29 EP EP10827521.5A patent/EP2493605A4/en not_active Withdrawn
- 2010-10-29 CN CN2010800498055A patent/CN102596394A/en active Pending
- 2010-10-29 JP JP2012537105A patent/JP2013509297A/en active Pending
- 2010-10-29 WO PCT/US2010/054680 patent/WO2011053770A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011053770A1 (en) | 2011-05-05 |
| US20110105316A1 (en) | 2011-05-05 |
| EP2493605A4 (en) | 2013-05-15 |
| CN102596394A (en) | 2012-07-18 |
| JP2013509297A (en) | 2013-03-14 |
| TW201130558A (en) | 2011-09-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100373572B1 (en) | Dehydrogenation catalyst and process | |
| JP5483114B2 (en) | A method for producing a multicomponent bismuth molybdate catalyst with pH adjustment and a method for producing 1,3-butadiene using the same. | |
| JP7113066B2 (en) | Fluid bed catalyst suitable for the preparation of halogenated aromatic nitriles, its preparation and use | |
| US20010025129A1 (en) | Processes for oxidative dehyrogenation | |
| KR20140108264A (en) | Zinc and/or manganese aluminate catalyst useful for alkane dehydrogenation | |
| WO2014051090A1 (en) | Oxide catalyst, method for producing same, and method for producing unsaturated aldehyde, diolefin or unsaturated nitrile | |
| CN101626833A (en) | A catalyst, its preparation and use | |
| TWI267401B (en) | A catalyst, its preparation and its use in a dehydrogenation process | |
| CN112812751A (en) | Heat storage material for propane dehydrogenation propylene preparation process and preparation method thereof | |
| JP2011178719A (en) | Process for producing butadiene | |
| KR101309259B1 (en) | Single crystalline catalyst of gamma-bismuth molybdate and process for preparing 1,3-butadiene using the catalyst | |
| US20100081855A1 (en) | Semi-Supported Dehydrogenation Catalyst | |
| JP2010527948A (en) | Oxidative dehydrogenation using boria-alumina catalyst | |
| WO2011053770A1 (en) | Designed mixed metal oxide ingredients for bulk metal oxide catalysts | |
| US11104623B2 (en) | Process for activating an aromatization catalyst | |
| JP3786437B2 (en) | Ethylbenzene dehydrogenation catalyst and production method thereof | |
| AU2003247653A1 (en) | A process for the dehydrogenation of an unsaturated hydrocarbon | |
| KR101229776B1 (en) | Complex oxide solid catalyst with core-shell structure and process for preparing 1,3-butadiene using the catalyst | |
| JP6973828B2 (en) | Method of filling catalyst and method of producing butadiene using this | |
| KR101158863B1 (en) | Core-shell solid catalyst and process for preparing 1,3-butadiene using the catalyst | |
| KR100863327B1 (en) | A solid catalyst with core-shell catalytic phase for preparing 1,3-butadiene | |
| JP4410954B2 (en) | Process for the production of highly active selective catalysts for the production of unsaturated nitriles | |
| JP2520279B2 (en) | Method for producing acrylonitrile | |
| CN114452981B (en) | Ethylbenzene dehydrogenation catalyst with ultralow water ratio and preparation method thereof | |
| CN119318967B (en) | Iron-based catalysts, their preparation methods and applications, and the FTO reaction |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20120426 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
| DAX | Request for extension of the european patent (deleted) | ||
| A4 | Supplementary search report drawn up and despatched |
Effective date: 20130411 |
|
| RIC1 | Information provided on ipc code assigned before grant |
Ipc: B01J 23/00 20060101ALI20130405BHEP Ipc: B01J 23/887 20060101ALI20130405BHEP Ipc: B01J 37/00 20060101ALI20130405BHEP Ipc: B01J 21/00 20060101AFI20130405BHEP |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 20130503 |